l-cysteine undergoes facile electron transfer with heteropoly 10-tungstodivanadophosphate,
[ \textPV\textV \textV\textV \textW 1 0 \textO 4 0 ]5 - , \left[ {{\text{PV}}^{\text{V}} {\text{V}}^{\text{V}} {\text{W}}_{ 1 0} {\text{O}}_{ 4 0} } \right]^{5 - } , at ambient temperature in aqueous acid medium. The stoichiometric ratio of [cysteine]/[oxidant] is 2.0. The products of the
reaction are cystine and two electron-reduced heteropoly blue, [PVIVVIVW10O40]7−. The rates of the electron transfer reaction were measured spectrophotometrically in acetate–acetic acid buffers at 25 °C.
The orders of the reaction with respect to both [cysteine] and [oxidant] are unity, and the reaction exhibits simple second-order
kinetics at constant pH. The pH-rate profile indicates the participation of deprotonated cysteine in the reaction. The reaction
proceeds through an outer-sphere mechanism. For the dianion −SCH2CH(NH3+)COO−, the rate constant for the cross electron transfer reaction is 96 M−1s−1 at 25 °C. The self-exchange rate constant for the
- \textSCH2 \textCH( \textNH3 + )\textCOO - \mathord
Lithium titanate ceramics doped with Eu were synthesized and their photoluminescence (PL) and emission spectral characteristics were investigated. PL spectra of the sample showed peaks corresponding to the 5D0→7FJ (J=0, 1, 2, 3 and 4) transitions under 230 nm excitation. The fluorescence lifetimes of Eu3+ ions were found out to be 645 μs. Strong red emission coming from the hypersensitive 5D0→7F2 transition of Eu3+ ion suggested the presence of the dopant ion in highly asymmetric environment. Further analysis of the emission spectrum revealed that the symmetry of the metal ion is very low i.e. C2. The emission intensity of the sample was compared with a commercial phosphor to get an idea about the commercial utility of the phosphor. Various emission properties for the system namely Judd-Ofelt intensity parameters, spontaneous emission probabilities, branching ratios, radiative lifetimes and quantum efficiency were evaluated for the dopant ion by adopting standard procedure. 相似文献
One of the objectives of coding theory is to ensure reliability of the computer memory systems that use high-density RAM chips with wide I/O data (e.g. 16, 32, 64 bits). Since these chips are highly vulnerable to m-spotty byte errors, this goal can be achieved using m-spotty byte error-control codes. This paper introduces the m-spotty Lee weight enumerator, the split m-spotty Lee weight enumerator and the joint m-spotty Lee weight enumerator for byte error-control codes over the ring of integers modulo ? (? ≥ 2 is an integer) and over arbitrary finite fields, and also discusses some of their applications. In addition, MacWilliams type identities are also derived for these enumerators. 相似文献
JPC – Journal of Planar Chromatography – Modern TLC - Piperine, an alkaloid with diverse biological activity commonly occurring in fruits of Piper sp., has high commercial, economical,... 相似文献
Synthesis of novel pyrroloisoquinoline and indolizinoindole derivatives with β-lactam unit has been achieved by sequential intermolecular 1,3-dipolar cycloaddition reaction and Pictet-Spengler cyclization. The azomethine ylide derived from β-lactam imine of α-amino ester in the presence of silver acetate reacted with nitrostyrenes to give pyrrolidinyl β-lactam, which underwent Pictet-Spengler cyclization in presence of trifluoroacetic acid to give pyrroloisoquinolines and indolizinoindoles. 相似文献
57Fe Mössbauer spectroscopy is used to study the interactions, geometry, and the coordination characteristics of the Fe-complexes of biopolymers such as chitosan, glucosamine, and chondritin sulfate. In addition, a computational effort is undertaken for predicting the geometries and energies of the metal complexes by the Density Functional Theory (DFT) methods as implemented in the Gaussian 2003 quantum mechanical program. Both experimental and computational results suggest that the structure of the metal complexes resemble closely the structure of the active sites of metalloenzymes in 2+ or 3+ oxidation states and is at least tetracoordinated and can possibly have six ligands. 相似文献
Single crystal EPR studies of Cu(II) incorporated in magnesium rubidium sulphate hexahydrate are carried out at RT and 77 K. Since the hyperfine lines are not resolved at RT, single crystal rotations have been carried out at 77 K. The spin Hamiltonian parameters calculated from the 77 K spectra are: g11=2.133, g22=2.137, g33=2.327, A11=0.01, A22=1.44 and . The impurity ion occupies an interstitial position in this crystal lattice, which is not very common for copper ion. In addition, the low hyperfine coupling constant is explained by considering an admixture of dx2-y2 ground state with dz2 excited state. Bonding parameters, κ=0.254, , α2=0.706, α=0.8406 have also been calculated. The present study has helped to understand the static nature of JT, for which the present system is an example. 相似文献